NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency
<jats:title>Abstract</jats:title><jats:p>The National Institute of Health (NIH) Library of integrated network-based cellular signatures (LINCS) program is premised on the generation of a publicly available data resource of cell-based biochemical responses or “signatures” to genetic...
Main Author: | Fraenkel, Ernest |
---|---|
Other Authors: | Massachusetts Institute of Technology. Department of Biological Engineering |
Format: | Article |
Language: | English |
Published: |
Springer Science and Business Media LLC
2023
|
Online Access: | https://hdl.handle.net/1721.1/147808 |
Similar Items
-
NeuroLINCS Proteomics: Defining human-derived iPSC proteomes and protein signatures of pluripotency
by: Andrea D. Matlock, et al.
Published: (2023-01-01) -
Systematic assessment of variability in the proteome of iPSC derivatives
by: Stephanie D. Beekhuis-Hoekstra, et al.
Published: (2021-10-01) -
Quantitative proteomic analysis of Rett iPSC-derived neuronal progenitors
by: Suzy Varderidou-Minasian, et al.
Published: (2020-05-01) -
Generation and proteome profiling of PBMC-originated, iPSC-derived lentoid bodies
by: Muhammad Ali, et al.
Published: (2020-07-01) -
Proteomic signatures of schizophrenia-sourced iPSC-derived neural cells and brain organoids are similar to patients' postmortem brains
by: Juliana Minardi Nascimento, et al.
Published: (2022-12-01)